The AAPS journal · 2005
Ajulemic acid (IP-751): synthesis, proof of principle, toxicity studies, and clinical trials.
СтатьяПоддержка NIH: внешняя программаПоддержка службы здравоохранения СШАОбзорНазвание и аннотация: Перевод пока не подготовлен
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Аннотация
Ajulemic acid (CT-3, IP-751, 1',1'-dimethylheptyl-Delta8-tetrahydrocannabinol-11-oic acid) (AJA) has a cannabinoid-derived structure; however, there is no evidence that it produces psychotropic actions when given at therapeutic doses. In a variety of animal assays, AJA shows efficacy in models for pain and inflammation. Furthermore, in the rat adjuvant arthritis model, it displayed a remarkable action in preventing the destruction of inflamed joints. A phase-2 human trial with chronic, neuropathic pain patients suggested that AJA could become a useful drug for treating this condition. Its low toxicity, particularly its lack of ulcerogenicity, further suggests that it will have a highly favorable therapeutic index and may replace some of the current anti-inflammatory/analgesic medications. Studies to date indicate a unique mechanism of action for AJA that may explain its lack of adverse side effects.
Предметные рубрики MeSH
AdultAnalgesicsAnimalsAnti-Inflammatory Agents, Non-SteroidalApoptosisArthritis, ExperimentalCannabinoidsCell Line, TumorClinical Trials, Phase II as TopicCytokinesDouble-Blind MethodDronabinolDrug Evaluation, PreclinicalEdemaFemaleGastritisHumansMaleMiceMiddle AgedMolecular StructureNeuralgiaRandomized Controlled Trials as TopicRats